Apoptosis-mimicking synthetic entities and use thereof in medical treatment

ABSTRACT

Synthetic and semisynthetic bodies having a three-dimensional structure, sized and shaped to resemble apoptotic cells and apoptotic bodies, and having phosphatidyl serine (PS) molecules on the surface thereof, are administered to a patient, to alleviate a variety of disorders such as T-cell mediated disorders (autoimmune conditions). The bodies are believed to trigger an apoptosis-like mechanism in the patient.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to Canadian Application Serial Number 2,319,928 filed Sep. 18, 2000.

FIELD OF THE INVENTION

This invention relates to synthetic and semi-synthetic compositions having biochemical activity, and to the uses thereof in the treatment and/or prophylaxis of various disorders in mammalian patients. More particularly, it relates to preparation and use of synthetic and semi-synthetic bodies which can mimic the process of cell apoptosis after introduction into the body of a patient, to produce beneficial effects.

BACKGROUND OF THE INVENTION

The following documents are cited herein:

1. Kerr, J. F. R., Wyllie A. H., Currie, A. R. (1992), “Apoptosis: a basic biological phenomenon with wide-ranging implications in tissue kinetics.” British Journal of Cancer 26: 239-257;

2. Fadok (1998) J. Clin. Invest., 101.890-898;

3. Fadok V. A., Voelker D. P., Campbell P. A., Cohen, J. J., Bratton, D. L., Henson, P. M. (1992), “Exposure of phosphatidylserine on the surface of apoptotic lymphocytes triggers specific recognition and removal by macrophages.” Journal of Immunology 148:2207-2216;

4. Fadok V. A., Bratton, D. L., Rose, D. M., Pearson, A., Exekewitz R. A. B., Henson, P. M. (2000), “A receptor for phosphatidylserine-specific clearance of apoptotic cells,” Nature 405:85-90;

5. Monastra et al. Neurology (1993) 48:153-163;

6. Zanotti et al., 1989;

7. Delwaide et al., (1986) Acta Neurol. Scand.; 73: 136-140.

8. Yechezkel Barenholz and Daan J. A. Chromeline, Liposomes as Pharmaceutical Dosage Forms, and literature cited therein, for example New, R. C., “Liposomes: A Practical Approach,” IRL Press at Oxford University Press, Oxford, England (1990), and Nassander, U. K., et al., In: “Biodegradable Polymers as Drug Delivery Systems” (M. Chasin and R. Langer, eds.) Marcel Dekker Inc., New York 1990, pages 261-338;

9. Griffin W S T, Stanley, L. C., Ling, C., White, L., Macleod, V. Perrot L. H J., White, C. L., Araoz, C., (1989), Brain interleukin 1 and S-100 immunoreactivity are elevated in Down's syndrome and Alzheimer's disease, Proceedings of the National Academy of Sciences USA 86: 7611-7615;

10. Mogi M., Harada, M., Narabayashi, H., Inagaki, H., Minami, M., Nagatsu T., (1996) “Interleukin (IL)-1 beta, IL-1, IL-4, IL-6 and transforming growth factor-alpha levels are elevated in ventricular cerebrospinal fluid in juvenile parkinsonism and Parkinson's disease,” Neuroscience Letters 211: 13-16;

11. Murray, C. A., Lynch, M. A., (1998) “Evidence that increase hippocampal expression of the cytokine interleukin-1β is a common trigger for age and tress-induced impairments in long-term potentiation,” Journal of Neuroscience 18:2974-2981;

12. Bliss, T. V. P., Collinridge, G. L., (1993) “A synaptic model of memory: long-term potentiation in the hippocampus,” Nature 361:31-39.

Two mechanisms of cell death in the body are recognized, necrosis and apoptosis. Apoptosis is the process of programmed cell death, described by Kerr et al. (1992) by which steady-state levels of the various organ systems and tissues in the body are maintained as continuous cell division is balanced by cell death. Cells undergoing apoptosis often exhibit distinct morphological changes such as pronounced decrease in cell volume, modification of the cytoskeletons resulting in pronounced membrane blebbing, a condensation of the chromatin, and degradation of the DNA into oligonucleosomal fragments. Following these morphological changes, an apoptotic cell may break up into a number of small fragments known as apoptotic bodies, consisting essentially of membrane-bound bodies containing intact organelles, chromatin etc. Apoptotic cells and apoptotic bodies are normally rapidly removed from the body by phagocytosis principally by macrophages and dendritic cells, before they can become lysed and release their potentially pro-inflammatory intracellular contents.

Macrophages which have ingested apoptotic cells and/or apoptotic bodies (e.g. phagocytosis) appear to inhibit pro-inflammatory cytokine production (Fadok et al., 1998) and thus may down-regulate a Th-1 response in a patient's immune system. Such down-regulation can also be achieved following injection of apoptotic cells or bodies, or following injection of cells susceptible to accelerated apoptosis.

During apoptosis, phosphatidylserine becomes exposed externally on the cell membrane (Fadok et al. (1992)) and this exposed phosphatidylserine binds to specific receptors to mediate the uptake and clearance of apoptotic cells in mammals (Fadok et al (2000)). The surface expression of phosphatidylserine on cells is a recognized method of identification of apoptotic cells.

Monastra et al. (1993) describe that the administration of phospholipid phosphatidylserine (PS) derived from bovine cortex (BC-PS) may have an effect on adoptively transferred Experimental Autoimmune Encephalomyelitis (EAE) in SJL/J mice. However, an extremely high dose of BC-PS, 30 mg/kg, was injected intraperitoneally on a daily basis. An equivalent dose of liposomes given to a human (greater than 2 grams per average individual) would be potentially toxic, expensive and therefore impractical and undesirable. Such quantities would be active, if at all, as drugs, and would be too large to act as immune system modifiers.

Oral administration of PS has been used both in animal models to improve spatial memory, in amounts of 50 mg/day (Zanotti et al., 1989), and in humans to treat Alzheimer's disease, in amounts of 300 mg/day (Delwaide et al., 1986) and showed statistically significant improvements in PS treated subjects as compared with placebo.

SUMMARY OF THE INVENTION

This invention is directed to the surprising discovery that PS-carrying bodies may be used to treat a number of diseases.

In particular, it is directed to a method for treating a T-cell function-mediated disorder comprising administering to a mammalian patient a non-toxic effective T-cell function-mediated disorder-treating amount of PS-carrying bodies wherein the progression of the T-cell function-mediated disorder is inhibited and/or symptoms of the disorder are reduced.

It is further directed to a method for treating an inflammatory disorder comprising administering to a mammalian patient a non-toxic effective inflammatory disorder-treating amount of PS-carrying bodies, wherein the progression of the inflammatory disorder are inhibited and/or symptoms of the disorder are reduced.

Yet another embodiment of this invention is a method for treating an endothelial function disorder comprising administering to a mammalian patient a non-toxic effective endothelial function disorder-treating amount of PS-carrying bodies, wherein the progression of the endothelial function disorder are inhibited and/or symptoms of the disorder are reduced.

Another embodiment is a method for treating an immune system disorder characterized by an inappropriate cytokine expression comprising administering to a mammalian patient a non-toxic effective inappropriate cytokine expression-treating amount of PS-carrying bodies, wherein the progression of the disorder are inhibited and/or symptoms of the disorder are reduced.

This invention is also directed to pharmaceutical compositions comprising pharmaceutically acceptable biocompatible synthetic or semi-synthetic bodies for administration to a mammalian patient and a pharmaceutically acceptable carrier, wherein at least a portion of said bodies have a conformation and size corresponding to mammalian apoptotic bodies wherein the surface of said bodies have been modified to contain a plurality of ligands for one or more phosphatidylserine receptors; which bodies are capable of binding to a phosphatidylserine receptor on an antigen presenting cell when administered to the mammalian patient. The biocompatible synthetic body may be a liposome.

Yet another embodiment of this invention is pharmaceutical compositions comprising a pharmaceutical carrier and biocompatible non-liposomal synthetic bodies for administration to a mammalian patient wherein the non-liposomal biocompatible synthetic bodies comprise pharmaceutically acceptable bodies have a conformation and size corresponding to mammalian apoptotic bodies wherein the surface of said pharmaceutically acceptable body has been modified to contain a plurality of ligands for one or more phosphatidylserine receptors; which biocompatible synthetic bodies are capable of binding to a phosphatidylserine receptor on an antigen presenting cell when administered to the mammalian patient. The biocompatible non-liposomal synthetic bodies may be selected from polysaccharides such as hydroxyethylcellulose, hydroxethyl starch, and agarose, polyethylene glycol, polyvinylprrolidone, polystyrene and a wide range of other natural, semi-synthetic and synthetic materials.

In another embodiment, this invention is directed to lyophilized or freeze-dried PS-carrying bodies and kits of parts containing lyophilized or freeze-dried PS-carrying bodies and a pharmaceutically acceptable carrier.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows net ear swelling (microns) in control and treated mice using the murine contact hypersensitivity (CHS) model.

FIG. 2 shows net ear swelling in control and treated mice in the CHS model where mice were treated with PS liposomes where the amount of PS in the liposome was varied.

FIG. 3 shows the change in ear swelling in control and treated mice where mice were treated with varying numbers of liposomes using the CHS model.

FIG. 4 shows the change in ear swelling in control and treated mice where mice were treated with varying sizes of PS-containing liposomes using the CHS model.

FIG. 5 shows the change in ear swelling in control and treated mice using the CHS model where agarose beads derivatized to carry PS on their surface were administered.

FIG. 6 is a bar graph showing the excitatory post-synaptic potential (epsp) slope (%) in control and treated rats using the Long-Term Potentiation (LTP) animal model.

FIG. 7 shows the concentration of IL-1β in the hippocampus of control and treated rats.

FIG. 8 shows reactive oxygen species (ROS) formation in the hippocampus of control and treated rats.

FIG. 9 shows the concentration of IL-10 in the hippocampus of control and treated rats.

DESCRIPTION OF THE INVENTION

According to the present invention, synthetic and semi-synthetic bodies which have the property of mimicking in vivo apoptotic cells and/or apoptotic bodies in that they are taken up by cells of the patient's immune system with accompanying beneficial effects such as inhibition of pro-inflammatory cytokines in vivo and/or promotion of anti-inflammatory cytokines are administered to patients. These synthetic and semi-synthetic bodies are three dimensional bodies having shapes and dimensions ranging from those resembling mammalian cells to shapes and dimensions approximating to apoptotic bodies produced by apoptosis of mammalian cells (typically but not exclusively spheroidal, cylindrical, ellipsoidal including oblate and prolate spheroidal, serpentine, reniform, etc., and from about 50 nanometers to about 500 microns in diameter), and having phosphatidyl serine (PS) molecules on the surface thereof. Such bodies are hereinafter referred to as “PS-carrying bodies.”

The term “synthetic or semi-synthetic PS-carrying bodies” refers to liposomes containing PS as well as up to 50% non-PS components of the liposomes. The term “non-liposomal synthetic bodies” refers PS-carrying bodies that are not liposomes.

As noted above, exposed PS on the membrane of a cell is known to play a key role in the clearance of apoptotic lymphocytes by macrophages. A receptor for PS is present on macrophages. A “phosphatidylserine receptor” or “PS receptor” is a receptor on an antigen presenting cell (APC), such as a macrophage, whose activity is blocked by soluble phosphatidylserine, either monomeric or oligomeric. It is contemplated that the PS receptor may also be present on other APCs, such as dendritic cells and B cells. It is understood that PS is a ligand of the PS receptor.

According to this invention, PS-carrying bodies interact with a patient's immune system, after administration to the patient by suitable means, presumably by engulfment by or other interaction with macrophages and/or dendritic cells or other antigen-presenting cells, to give substantially similar effects in terms of cytokine responses as are obtained when apoptotic cells/bodies are phagocytosed by macrophages.

It is also significant that, in the present invention, PS-carrying bodies are acting as modifiers of the patient's immune system, in a manner somewhat similar to that of a vaccine. Accordingly, they are used in quantities and by administration methods to provide a sufficient localized corcentration of the PS-carrying bodies at the site of injection to initiate the appropriate immune response. Quantities of PS-carrying bodies appropriate for immune system modifying substances are generally not directly correlated with body size of the recipient animal and can, therefore, be clearly distinguished from drug dosages, which are designed to provide therapeutic levels of active substances in a patient's bloodstream and tissues. Drug dosages and are accordingly very much larger.

It is contemplated that the patient may be a mammal, including but not limited to, humans and domestic animals such as cows, horses, pigs, dogs, cats, and the like.

PS-carrying bodies have surface PS molecules. As a phospholipid, PS can form the membrane of a liposome, either as the sole constituent of the membrane or as a major or minor component thereof, with other phospholipids and/or membrane forming materials. Liposomes, or lipid vesicles, are sealed sacs, in the micron or sub-micron range, the walls of which consist of layers of suitable amphiphiles. They normally contain an aqueous medium. It is understood that the PS-carrying body is not limited to a liposomal structure.

Phospholipids are amphiphilic molecules (i.e. amphiphiles), meaning that the compound comprises molecules having a polar water-soluble group attached to a water-insoluble hydrocarbon chain. The amphiphiles serving as the layers of the matrix have defined polar and apolar regions. The amphiphiles can include naturally occurring lipids such as PS, phosphatidylethanolamine, phosphatidylinositol, phosphatidylcholine, cholesterol, cardiolipin, ceramides and sphingomyelin, used alone or in admixture with one another. They can be synthetic compounds such as polyoxyethylene alkylethers, polyoxyethylene alkylesters and saccharosediesters.

The present invention contemplates the use, as PS-carrying bodies, not only those liposomes having PS as a membrane constituent, but also liposomes having non-PS membrane substituents which carry on their external surface molecules of phosphoserine, either monomers or oligomers (as distinguished from phosphatidylserine), e.g., chemically attached by chemical modification of the liposome surface, making the PS available for subsequent interaction with components of the patient recipient's immune system. Because of the inclusion of phosphoserine on the surface of such molecules, they are included within the definition of PS-carrying bodies.

Preferred PS-carrying bodies used in the present invention are liposomes constituted to the extent of 50% -100% by weight of phosphatidylserine (PS), the balance being phosphatidylcholine (PC) or other such biologically acceptable phospholipid(s). More preferred are liposomes constituted by PS to the extent of 65% -90% by weight, most preferably 70% -80% by weight, with the single most preferred embodiment, on the basis of current experimental experience, being PS 75% by weight, the balance being other phospholipids such as PC. They are prepared from mixtures of the appropriate amounts of phospholipids as starting materials, by known methods.

Methods of preparing liposomes of the appropriate size are known in the art and do not form part of this invention. Reference may be made to various textbooks and literature articles on the subject, for example, the review article by Yechezkel Barenholz and Daan J. A. Chromeline, and literature cited therein, for example New, R. C. (1990), and Nassander, U. K., et al. (1990).

The diameter of the PS liposomes of the preferred embodiment of this invention is from about 50 nanometers to about 1000 nanometers, more preferably from about 50 nanometers to about 500 nanometers. Such preferred diameters will correspond to the diameters of mammalian apoptotic bodies.

Various alternatives to liposomes may be used as PS-carrying bodies in the present invention. These include particles, granules, microspheres or beads of biocompatible materials, natural or synthetic, such as polyethylene glycol, polyvinylprrolidone, polystyrene, etc., polysaccharides such as hydroxethyl starch hydroxyethylcellulose, agarose and the like, as commonly used in the pharmaceutical industry. Some such suitable substances for derivatization to attach the PS and, in the case of agarose, with PS attached, are commercially available, e.g. from Polysciences, Inc. 400 Valley Road, Warrington, Pa. 18976, or from Sigma Aldrich Fine Chemicals. The beads may be solid or hollow, or filled with biocompatible material. They are modified as required so that they carry PS molecules on their surfaces.

The PS-carrying bodies may be administered to the patient by any suitable means which brings them into operative contact with active ingredients of the patient's immune system.

The PS-carrying bodies may be suspended in a pharmaceutically acceptable carrier, such as physiological sterile saline, sterile water, pyrogen-free water, isotonic saline, and phosphate buffer solutions, as well as other non-toxic compatible substances used in pharmaceutical formulations. Preferably, the PS-carrying bodies are constituted into a liquid suspension in a biocompatible liquid such as physiological saline and administered to the patient in any appropriate route which introduces it to the immune system, such as intra-arterially, intravenously or most preferably intramuscularly or subcutaneously.

It is contemplated that the PS-carrying bodies may be freeze-dried or lyophilized which may be later resuspended for administration. This invention is also directed to a kit of part comprising lyophilized or freeze-dried PS-carrying bodies and a pharmaceutically acceptable carrier, such as physiological sterile saline, sterile water, pyrogen-free water, isotonic saline, and phosphate buffer solutions, as well as other non-toxic compatible substances used in pharmaceutical formulations.

A preferred manner of administering the PS-carrying bodies to the patient is a course of injections, administered daily, several times per week, weekly or monthly to the patient, over a period ranging from a week to several months. The frequency and duration of the course of the administration is likely to vary from patient to patient, and according to the condition being treated, its severity, and whether the treatment is intended as prophylactic, therapeutic or curative. Its design and optimization is well within the skill of the attending physician.

The quantities of PS-carrying bodies to be administered will vary depending on the nature of the mammalian disorder it is intended to treat and on the identity and characteristics of the patient. It is important that the effective amount of PS-bodies is non-toxic to the patient, and is not so large as to overwhelm the immune system. When using intra-arterial, intravenous, subcutaneous or intramuscular administration of a liquid suspension of PS-carrying bodies, it is preferred to administer, for each dose, from about 0.1-50 ml of liquid, containing an amount of PS-carrying bodies generally equivalent to 10% -1000% of the number of leukocytes normally found in an equivalent volume of whole blood or the number of apoptotic bodies that can be generated from them. Generally, the number of PS-carrying bodies administered per delivery to a human patient is in the range from about 500 to aboat 500,000,000 (<50 ng lipid), more preferably from about 10,000 to about 10,000,000, and most preferably from about 200,000 to about 2,000,000.

Since the PS-carrying bodies are acting, in the process of the invention, as immune system modifiers, in the nature of a vaccine, the number of such bodies administered to an injection site for each administration is a more meaningful quantitation than the number or weight of PS-carrying bodies per unit of patient body weight. For the same reason, it is now contemplated that effective amounts or numbers of PS-carrying bodies for small animal use may not directly translate into effective amounts for larger mammals on a weight ratio basis.

While it is not intended that the scope of the present invention should be limited by any particular theories of its mode of operation, the following is offered as a tentative explanation, for a better understanding of the ways an means by which the invention may be put into practice. It is postulated that antigen-presenting cells of the patient's immune system, notably professional antigen presenting cells (APCs) including macrophages and dendritic cells, take up the PS-carrying bodies in a similar manner to the way in which they would take up apoptotic cells an apoptotic bodies. Having taken up the PS-carrying bodies, the APCs induce an anti-inflammatory response promoting a change in the Th cell population with an increase in the proportion of Th2 cells and/or other regulatory/anti-inflammatory cell populations (e.g., Tr1 cells), and a decrease in Th1 cells. Th2 cells and other regulatory cells secrete anti-inflammatory cytokines such as interleukin-10, leading to reduced inflammation.

The present invention is indicated for use in prophylaxis and/or treatment of a wide variety of mammalian disorders where T-cell function, inflammation, endothelial dysfunction and inappropriate cytokine expression are involved. A patient having or suspected of having such a disorder may be selected for treatment. “Treatment” refers to a reduction of symptoms, such as, but not limited to, a decrease in the severity or number of symptoms of the particular disease or to limit further progression of symptoms.

With respect to T-cell function (T-cell mediated) disorders, these may be autoimmune disorders including, but not limited to diabetes, scleroderma, psoriasis and rheumatoid arthritis.

The invention is indicated for use with inflammatory allergic reactions, organ and cell transplantation reaction disorders, and microbial infections giving rise to inflammatory reactions. It is also indicated for use in prophylaxis against oxidative stress and/or ischemia reperfusion injury, ingestion of poisons, exposure to toxic chemicals, radiation damage, and exposure to airborne and water-borne irritant substances, etc., which cause damaging inflammation. It is also indicated for inflammatory, allergic and T-cell-mediated disorders of internal organs such as kidney, lever, heart, etc.

With respect to disorders involving inappropriate cytokine expression for which the present invention is indicated, these include neurodegenerative diseases. Neurodegenerative diseases, including Down's syndrome, Alzheimer's disease and Parkinson's disease, are associated with increased levels of certain cytokines, including interleukin-1β (IL-1β) (see Griffin WST et al. (1989); Mogi M. et al. (1996)). It has also been shown that Il-1β inhibits long-term potentiation in the hippocampus (Murray, C. A. et al. (1998)). Long-term potentiation in the hippocampus is a form of synaptic plasticity and is generally considered to be an appropriate model for memory and learning (Bliss, T. V. P. et al. (1993)). Thus, inappropriate cytokine expression in the brain is currently believed to be involved in the development and progression of neurodegenerative diseases.

Thus, the invention is indicated for the treatment and prophylaxis of a wide variety of mammalian neurodegenerative and other neurological disorders, including Downs syndrome, Alzheimer's disease, Parkinson's disease, senile dementia, depression, multiple sclerosis, Huntingdon's disease, peripheral neuropathies, spinal cord diseases, neuropathic joint diseases, chronic inflammatory demyelinating disease, neuropathies including mononeuropathy, polyneuropathy, symmetrical distal sensory neuropathy, neuromuscular junction disorders, myasthenias and amyotrophic lateral sclerosis (ALS).

Regarding disorders involving endothelial dysfunction, the present invention is indicated for the treatment and prophylaxis of a wide variety of such mammalian disorders including, but not limited to, cardiovascular diseases, such as atherosclerosis, peripheral arterial or arterial occlusive disease, congestive heart failure, cerebrovascular disease (stroke), myocardial infarction, angina, hypertension, etc., vasospastic disorders such as Raynaud's disease, cardiac syndrome X, migraine etc., and the damage resulting from ischemia (ischemic injury or ischemia-reperfusion injury). In summary, it can be substantially any disorder that results from an inappropriately functioning endothelium.

EXAMPLES 1-5

These examples show the effect of injecting various phosphatidylserine-containing liposomes of various sizes and compositions, and in various concentrations, on ear swelling in the murine contact hypersensitivity (CHS) model, a Th1-mediated inflammatory reaction, an art-accepted model. For these experiments, female BALB/c mice (Jackson Laboratories) age 6-8 weeks and weighing 22-25 g were used.

EXAMPLE 1 PS Liposomes

Phosophatidylserine (PS) containing liposomes of size 100±20 nanometers were prepared as described above which had a phosphatidylserine content of 100% (i.e. made entirely of PS). A stock suspension of liposomes containing 4.8×10¹⁴ liposomes per ml was diluted with PBS to give an injection suspension containing 6×10⁶ particles per ml, and each animal was injected with 50 μl of this suspension, containing 3×10⁵ liposomes.

Protocol

Test group A which received the liposomes comprised 25 animals in number. Control group comprised 24 animals. The following experiments were run: TABLE 1 Day 7 Group Day 1 Day 2 Day 3 Day 4 Day 5 Day 6 (24 hours) A Inject Inject Inject Inject Inject Inject Ear measured 100% then then PS sensitize challenge positive sensitized challenge Ear measured control (untreated animals)

On Days 1-6, mice of Group A were injected with liposomes prepared from 100% PS. Liposomes were injected in 50 μl volume via intramuscular (IM) injection, i.e. 300,000 liposomes per injection, for a total administration over the test period of 1,800,000 liposomes. Mice of the control group received no liposomes, but were sensitized, challenged axd tested in the same way as mice of group A, as described below.

Sensitization

On Day 1, following liposome injection for that day, mice were anesthetized using 0.2 ml intraperitoneal (IP) injection of 5 mg/ml pentobarbital sodium. The abdominal skin of the mouse was sprayed with 70% ETOH. A blade was used to remove about a one-inch diameter of hair from the abdomen. The bare area was painted with 25 μl of 0.5% 2,4-dinitrofluorobenzene (DNFB) in 4:1 acetone:olive oil using a pipette tip.

Challenge

On Day 6, following liposome injection for that day, mice were challenged with DNFB as follows: 10 μl of 0.2% DNFB was painted on the dorsal surface of the right ear with a pipette tip and 10 μl of vehicle was painted on the left ear with a pipette tip.

Results

On Day 7, 24 hours after challenge, each animal was anesthetized with Halothane, and ear thickness (in microns) was measured using a Peacock spring loaded micrometer. Increase in ear swelling is used as a measure of CHS response. Data is expressed as the difference in the treated right ear thickness minus the thickness of the vehicle treated left ear. The significance of difference between the two experimental groups is determined by the two-tailed student test. A value of p<0.05 is considered significant. The results are presented below, and are also presented graphically on accompanying FIG. 1, a bar graph of ear swelling, in microns. Group Control A Mean ear swelling 10.75 8.52 (microns) Standard deviation 3.03 2.77 Standard error 0.62 0.55 P vs. control <0.01 % inhibition vs. 20.70 control

EXAMPLE 2

Liposomes of size 100±20 nanometers and containing different amounts of phosphatidyl serine, namely 90%; 75% and 50%, with the remainder being phosphatidylcholine (PC), were prepared as described, from starting mixtures of the appropriate relative quantities of the respective phospholipids. Using 4 different groups of animals, five mice per group, the following experiments were run. Day 7 Group Day 1 Day 2 Day 3 Day 4 Day 5 Day 6 (24 hours) B Inject Inject Inject Inject Inject Inject Ear measured 90% PS then then sensitize challenge C Inject Inject Inject Inject Inject Inject Ear measured 75% PS then then sensitize challenge D Inject Inject Inject Inject Inject Inject Ear measured 50% PS then then sensitize challenge positive sensitized challenged Ear measured control (untreated animals The amounts and procedure for injection, the sensitization procedure, the challenge procedure and the results measurements were all as described in Example 1.

The results are given below, in Table 2, and are graphically presented on FIG. 2. They show an apparent optimum PS concentration in the liposome of about 75% by weight. TABLE 2 Group B C D Control % PS liposome 90 75 50 — Mean swelling 7.33 5.53 6.87 10.43 Standard deviation 2.50 3.60 2.26 3.32 Standard error 0.67 0.96 0.60 0.86 P vs. control 0.00829 0.000757 0.002135 % inhibition 29.7 47 34.1 vs. control

EXAMPLE 3

Again using the CHS murine model described above, liposomes of size 100±20 nanometers and containing 75% PS and 25% PC were injected into groups of mice according to the same protocol but at different dosage amounts i.e. different numbers of liposomes in each 50 μl injection. The numbers of liposomes per ml for the respective groups of animals, and the results obtained, using the same test and measurement procedures, were as follows:

Group E-10¹⁰ (10 animals) average net ear swelling 11.10; SD 2.56; SE 0.81;

-   -   % of control 86; % reduction 14;     -   p vs control 0.052

Group F-10⁸ (15 animals) average net ear swelling 8.93; SD 2.49; SE 0.64;

-   -   % of control 68; % reduction 32;     -   p vs control <0.0001

Group G-10⁷ (5 animals) average net ear swelling 6.20; SD 1.92; SE 0.86;

-   -   % of control 48; % reduction 52;     -   p vs. control <0.0001

Group H-10⁶(15 animals) average net ear swelling 5.13; SD 2.17; SE 0.56;

-   -   % of control 40; % reduction 60;     -   p vs. control <0.0001

Group J-10⁵ (5 animals) average net ear swelling 7.60; SD 1.52; SE 0.68;

-   -   % of control 59; % reduction 41;     -   p vs. control <0.0001

Group K-10⁴(10 animals) average net ear swelling 10.0; SD 1.05; SE 0.33;

-   -   % of control 78; % reduction 22;     -   p vs. control 0.000128.

These results are presented graphically on FIG. 3

EXAMPLE 4

Liposomes of 100% PS of various sizes were prepared, and injected into groups of mice according to the protocol described in Example 1. The volumes of injection, numbers of liposomes per injection, procedures and measurements were also as described in Example 1.

The results obtained were as follows: Group average ear (3 animals Liposome swelling, % each) size (nm) of control SD SE L 50 23 1.00 0.45 M 100 28 2.00 0.89 N 400 25 5.13 2.29

These results are presented graphically on accompanying FIG. 4. The liposomes are of fairly uniform size, with an approximate size range of ±20 nm.

EXAMPLE 5

Agarose beads derivatized to carry phosphatidylserine PS on their surfaces were used in the murine contact hypersensitivity model described in Example 1, in place of the liposomes. The agarose beads were characterized by an average particle size of 45-165 microns and generally spherical in size (Sigma Aldrich Fine Chemical, Catalogue no. P3578) As a control, similar agarose beads free of PS were used (Sigma Aldrich Fine Chemical, Catalogue no. A9045). Both the derivatized and the non-derivatized beads are commercially available from Sigma Chemical Co.

The agarose beads were suspended in PBS, and injected into the animals at a dosage of 300,000 beads, in 50 μl of suspension for each injection, according to the procedures and protocol described in Example 1. Measurements of ear swelling were taken as described. Five animals were used, in each of the experimental group and the control group.

Whereas the animals receiving underivatized agarose showed a mean net change in ear thickness as a result of the experiment of 7.8 μm (SD 2.17, SEM 0.97), the corresponding number for the animals receiving PS-derivatized beads was 4.00 (SD 2.92, SEM 1.30, p vs agarose 0.047509), indicating significant activity of PS when attached to solid beads in accordance with the invention, as well as liposomal forms thereof. The results are presented graphically in FIG. 5.

EXAMPLE 6

The hippocampus of the brain has been identified as a brain area which is especially vulnerable in degenerative conditions associated with cognitive dysfunction, such as Alzheimer's disease. In order to study the cellular and molecular mechanisms underlying cognitive function, the Long-Term Potentiation (LTP) animal model is used. LTP is a form of synaptic plasticity that occurs in the hippocampal formation which has been proposed as a biological substrate for learning and memory (Bliss et al, Nature 361:31-39 (1990)). Flectrophysiology recording of LTP in rats in vivo followed by analysis of biochemical changes in hippocampal tissue harvested following recording provides a model which permits investigation of how the cellular events that underlie LTP may be altered in states associated with neuroinflammation such as aging, stress, Alzheimer's disease, and bacterial infection.

Systemic administration of lipopolysaccharide (LPS), a component of the cell wall of Gram-negative bacteria, provokes an activation of the immune system by inducing an increase in pro-inflammatory cytokines such as IL-1β. One example of a neuronal deficit induced by LPS and IL-1β is the impairment of long term potentiation (LTP) in the hippocampus. An indicator of LTP is the mean slope of the population excitatory post-synaptic potential (epsp). Upon tetanic stimulation, the epsp slope (%) rises sharply indicating increased synaptic activity, but LPS-induced inhibition of LTP lessens this rise, and/or causes the epsp slope to revert more rapidly to base line, indicating that the increased sypnaptic activity is short-lived. Accordingly measurements of the epsp slope (%) at timed intervals after tetanic stimulation can be used to reflect memory and the loss thereof following an inflammatory stimulus as well as inflammation in the hippocampus of the brain.

Protocol

LTP: 6 groups of 8 Male Wistar rats (c.300 g) were injected intramuscularly with saline carrier alone or with PS bodies, namely liposomes of 100% PS, size 100±20 nanometers in saline carrier. 9×10⁵ liposomes in 150 μl of saline were injected into the rats on days −14, −13, and −1.

On day 0, rats were anesthetized with urethane (1.5 mg/kg, ip) and injected with LPS (lipopolysaccharide) (100 mg/kg i.p.) or saline as a control. After three hours, a bipolar stimulating electrode and a unipolar recording electrode were implanted in the perforant path and in the dorsal cell body of the dentate gyrus respectively. 0.033 Hz test shocks were given and responses recorded for 10 minutes before and 45 minutes after tetanic stimulation (3 trains of stimuli delivered at 30 sec. intervals, 250 Hz for 200 ms) to induce LPS.

The rats were killed by decapitation; the hippocampus, the tetanized and untetanized dentate gyri, the cortex and entorhinal cortex were dissected on ice, cross-chopped into slices and frozen in 1 ml of Krebs solution containing 10% DMSO.

Effectiveness of blocking LPS-induced inhibition of LTP was assessed from the electrophysiological recordings of neurotransmitter release in the tissue. The epsp slope (%) was followed for 10 minutes before and 40 minutes after tetanic stimulation. Tissue from animals which had received a course of pretreatment with PS liposomes and an injection of LPS exhibited a decline in epsp slope (%) of less than 5% at 40 to 45 minutes after tetanic stimulation, whereas tissue from similarly injected animals without the PS liposome. pretreatment course showed an approximate 25% reduction over the same period. This is a clear indication the described pre-treatment with PS liposomes is exerting a neuroprotective effect. This is shown in FIG. 6, bar graphs of epsp slope (%) of LPS-injected, pretreated animal tissues (right hand side) and LPS-injected, non-pretreated animal tissues (left hand side), at 40-45 minutes from tetanic stimulation). The ** notation indicates significant difference from the respective saline control. The ++ notation indicates significant difference from the LPS injected, non-pre-conditioned control.

In addition, IL-1β concentration in the hippocampus was measured, by enzyme-linked immunosorbent assay techniques known in the art. The results are shown in FIG. 7, bar graphs of IL-1β in pg/mg for control tissues which received no pretreatment with PS liposomes (left hand side) and tissues which received the pre-treatment described above (right hand side). The shaded bars represent results from tissues of animals given an LPS injection, the clear bars those which received no such injection. It is clear that the preconditioning treatment has effectively inhibited the up-regulation of the inflammatory cytokine IL-1β ordinarily resulting from LPS injection.

Similarly, reactive oxygen species (ROS) formation in the hippocampus was investigated. ROS was assessed in synaptosomes prepared from hippocampus by measuring DCF, the oxidized fluorescent product of DCFH-DA. ROS are known to destroy nerve cells. These results are similarly presented in FIG. 8, again demonstrating the neuroprotective effect of the process of the present invention.

Further, the concentration of the anti-inflammatory cytokine IL-10 in the hippocampus was measured. IL-10 concentration was measured by enzyme-linked immunosorbent assay, and expressed as a percentage difference from the control. These results are presented, in a similar manner as FIGS. 7 and 8, in FIG. 9. They show that, in tissue from animals which had not received pre-treatment according to the invention, LPS injection caused a reduction in IL-10 content of about 30% (left side bars) as compared with saline injection. In contrast, in tissue from animals subjected to the course of pre-treatment with PS liposomes as described, LPS treatment caused an increase of about 45% in the IL-10 content as compared with saline injection (right side bars).

These results on IL-10 and IL-1β contents indicate significant anti-inflammatory effects in the hippocampus, following pre-treatment in accordance with the present invention.

In summary, the results show that PS-carrying bodies are effective to block LPS-induced LTP inhibition and neuroinflammation.

All publications, patents and patent applications previously cited above are herein incorporated by reference in their entirety. 

1-46. (canceled)
 47. A method for treating an inflammatory disorder comprising administering to a mammalian patient a non-toxic effective inflammatory disorder-treating amount of PS-carrying bodies, wherein progression of the inflammatory disorder is inhibited and/or the symptoms of the disorder are reduced.
 48. The method of claim 47 wherein the inflammatory disorder is selected from the group consisting of inflammatory allergic reactions, organ and cell transplantation reaction disorders, microbial infections giving rise to inflammatory disorders, oxidative stress and/or ischemia reperfusion injury, ingestion of poisons, exposure to toxic chemicals, radiation damage, exposure to airborne and water-borne irritant substances that cause damaging inflammation, inflammatory disorders of internal organs, and allergic disorders of internal organs.
 49. The method of claim 48 wherein the inflammatory disorder is an inflammatory or allergic disorder of the kidney, the liver, or the heart.
 50. The method of claim 48 wherein the amount of PS-carrying bodies administered is from about 500 to about 500,000,000 bodies.
 51. The method of claim 50 wherein the amount of PS-carrying bodies administered is from about 10,000 to about 10,000,000 bodies.
 52. The method of claim 50 wherein the amount of PS-carrying bodies administered is from about 200,000 to about 2,000,000 bodies.
 53. The method of claim 48 wherein the PS-carrying bodies comprise from about greater than 65% PS.
 54. The method of claim 53 wherein the PS-carrying bodies comprise from about 65% to about 90% PS.
 55. The method of claim 53 wherein the PS-carrying bodies comprise from about 70% to about 80% PS.
 56. The method of claim 53 wherein the PS-carrying bodies comprise about 75% PS.
 57. The method of claim 53 wherein the PS-carrying bodies are liposomes.
 58. The method of claim 53 wherein said PS-carrying bodies are biocompatible non-liposomal synthetic bodies.
 59. A method for treating an endothelial function disorder comprising administering to a mammalian patient a non-toxic effective endothelial function disorder-treating amount of PS-carrying bodies, wherein progression of the endothelial function disorder is inhibited and/or the symptoms of the disorder are reduced.
 60. The method of claim 59 wherein the endothelial function disorder is selected from the group consisting of cardiovascular diseases, vasospastic disorders, and damage resulting from ischemia.
 61. The method of claim 59 wherein the endothelial function disorder is selected from the group consisting of atherosclerosis, peripheral arterial or arterial occlusive disease, congestive heart failure, cerebrovascular disease (stroke), myocardial infarction, angina, and hypertension.
 62. The method of claim 59 wherein the endothelial function disorder is selected from the group consisting of Raynaud's disease, cardiac syndrome X, and migraine.
 63. The method of claim 59 wherein the endothelial function disorder is ischemic injury or ischemia-reperfusion injury.
 64. The method of claim 59 wherein the amount of PS-carrying bodies administered is from about 500 to about 500,000,000 bodies.
 65. The method of claim 59 wherein the amount of PS-carrying bodies administered is from about 10,000 to about 10,000,000 bodies.
 66. The method of claim 59 wherein the amount of PS-carrying bodies administered is from about 200,000 to about 2,000,000 bodies.
 67. The method of claim 59 wherein the PS-carrying bodies comprise from about greater than 65% PS.
 68. The method of claim 67 wherein the PS-carrying bodies comprise from about 65% to about 90% PS.
 69. The method of claim 67 wherein the PS-carrying bodies comprise from about 70% to about 80% PS.
 70. The method of claim 67 wherein the PS-carrying bodies comprise about 75% PS.
 71. The method of claim 67 wherein the PS-carrying bodies are liposomes.
 72. The method of claim 67 wherein said PS-carrying bodies are biocompatible non-liposomal synthetic bodies.
 73. A method for treating an immune system disorder characterized by an inappropriate cytokine expression comprising administering to a mammalian patient a non-toxic effective inappropriate cytokine expression-treating amount of PS-carrying bodies, wherein progression of the disorder is inhibited and/or the symptoms of the reduced.
 74. The method of claim 73 wherein the immune system disorder characterized by an inappropriate cytokine expression is a neurodegenerative disease or a neurological disorder.
 75. The method of claim 74 wherein the neurodegenerative disease or neurological disorder is selected from the group consisting of Down's syndrome, senile dementia, depression, multiple sclerosis, Huntingtdon's disease, peripheral neuropathies, spinal cord disease, neuropathic joint diseases, chronic inflammatory demyelinating disease, neuropathies including mononeuropathy, polyneuropathy, symmetrical distal sensory neuropathy, neuromuscular junction disorders, myasthenias and amyotrophic lateral sclerosis (ALS).
 76. The method of claim 74 wherein the neurodegenerative disease is Alzheimer's disease or Parkinson's disease.
 77. The method of claim 74 wherein the amount of PS-carrying bodies administered is from about 500 to about 500,000,000 bodies.
 78. The method of claim 74 wherein the amount of PS-carrying bodies administered is from about 10,000 to about 10,000,000 bodies.
 79. The method of claim 74 wherein the amount of PS-carrying bodies administered is from about 200,000 to about 2,000,000 bodies.
 80. The method of claim 74 wherein the PS-carrying bodies comprise from about greater than 65% PS.
 81. The method of claim 80 wherein the PS-carrying bodies comprise from about 65% to about 90% PS.
 82. The method of claim 80 wherein the PS-carrying bodies comprise from about 70% to about 80% PS.
 83. The method of claim 80 wherein the PS-carrying bodies comprise about 75% PS.
 84. The method of claim 74 wherein the PS-carrying bodies are liposomes.
 85. The method of claim 74 wherein said PS-carrying bodies are biocompatible non-liposomal synthetic bodies.
 86. A pharmaceutical composition comprising a pharmaceutical carrier and biocompatible non-liposomal synthetic bodies for administration to a mammalian patient wherein the non-liposomal biocompatible synthetic bodies comprise pharmaceutically acceptable bodies have a conformation and size corresponding to mammalian apoptitic bodies wherein the surface of said pharmaceutically acceptable body has been modified to contain a plurality of ligands for one or more phosphatidylserine receptors; which biocompatible synthetic bodies are capable of binding to a phosphatidylscrine receptor on an antigen presenting cell when administered to the mammalian patient.
 87. The pharmaceutical composition of claim 86 wherein the biocompatible non-liposomal synthetic body is selected from hydroxyethylcellulose, polyethylene glycol, hydroxethyl starch, polyvinylpyrrolidone, polysaccharides, polystyrene and agarose.
 88. The pharmaceutical composition of claim 86 wherein said biocompatible non-liposomal synthetic bodies have a diameter of about 50 nanomenters—500 microns.
 89. The pharmaceutical composition of claim 88 wherein said biocompatible non-liposomal synthetic bodies have a diameter of about 50 nanomenters—1000 nanometers.
 90. The pharmaceutical composition of claim 86 comprising a unit dosage form.
 91. A process for alleviating the symptoms of a disorder in a mammalian patient, which comprises administering to the patient an effective amount of PS-carrying bodies as defined herein, wherein the disorder is an inflammatory disorder, an endothelial dysfunction disorder or an inappropriate cytokine expression disorder.
 92. Lyophilized or freeze dried PS-carrying bodies.
 93. A kit of parts comprising the lyophilized or freeze dried PS-carrying bodies of claim 46 and a pharmaceutically acceptable carrier.
 94. The kit of claim 93 wherein the pharmaceutically acceptable carrier is selected from physiological sterile saline, sterile water, pyrogen-free water, isotonic saline, and phosphare buffer solution. 